Synthesis, Characterization and Properties of Antibacterial Polyurethanes

Novel physically crosslinked polyurethane (PUII), based on isophorone diisocyanates, was prepared by a conventional two-step method. The chemical structures of the PUII were characterized by fourier transform infrared (FTIR), proton nuclear magnetic resonance (1H NMR), gel permeation chromatography (GPC), scanning electron microscopy (SEM) and DSC. The PUII hydrogels were subjected to solvent-induced self-assembly in THF + water to construct a variety of morphologies. The self-assembly morphology of the PUII was observed by scanning electron microscopy (SEM). The PUII films with different amounts (0.2%, 0.4%, 0.6%, 0.8%, 1.0%) of 1,3,5-Tris(2-hydroxyethyl)hexahydro-1,3,5-triazine (TNO) were challenged with Escherichia coli, Staphylococcus aureus, Bacillus subtilis and Gray mold. The results showed that when a small amount of antibacterial agent were added, the antibacterial effect of films on Botrytis cinerea was more obvious. The mechanical evaluation shows that the antimicrobial polyurethane films exhibit good mechanical properties.

Organ-Specific Metabolome Deciphering Cell Pathways to Cope with Mercury in Wild Fish (Golden Grey Mullet Chelon auratus)

Metabolomics is a powerful approach in evaluating the health status of organisms in ecotoxicological studies. However, metabolomics data reflect metabolic variations that are attributable to factors intrinsic to the environment and organism, and it is thus crucial to accurately evaluate the metabolome of the tissue/organ examined when it is exposed to no stressor. The metabolomes of the liver and gills of wild golden grey mullet (Chelon auratus) from a reference area were analyzed and compared by proton nuclear magnetic resonance (1H NMR)-based metabolomics. Both organs were characterized by amino acids, carbohydrates, osmolytes, nucleosides and their derivatives, and miscellaneous metabolites. However, similarities and differences were revealed in their metabolite profile and related to organ-specific functions. Taurine was predominant in both organs due to its involvement in osmoregulation in gills, and detoxification and antioxidant protective processes in liver. Environmental exposure to mercury (Hg) triggered multiple and often differential metabolic alterations in fish organs. Disturbances in ion-osmoregulatory processes were highlighted in the gills, whereas differential impairments between fish organs were pointed out in energy-producing metabolic pathways, protein catabolism, membrane stabilization processes, and antioxidant defense system, reflecting the induction of organ-specific adaptive and defensive strategies. Overall, a strict correlation between metabolites and organ-specific functions of fish gills and liver were discerned in this study, as well as organ-specific cytotoxicity mechanisms of Hg in fish.

NMR Hydrophilic Metabolomic Analysis of Bacterial Resistance Pathways using Multivalent Antimicrobials with Challenged and Unchallenged Wild Type and Mutated Gram-Positive Bacteria

Multivalent membrane disruptors are a relatively new antimicrobial scaffold that are difficult for bacteria to develop resistance to and can act on both Gram-positive and Gram-negative bacteria. Proton Nuclear Magnetic Resonance (1H NMR) metabolomics is an important method for studying resistance development in bacteria, since this is both a quantitative and qualitative method to study and identify phenotypes by changes in metabolic pathways. In this project, the metabolic differences between wild type Bacillus cereus (B. cereus) samples and B. cereus that was mutated through 33 growth cycles in a nonlethal dose of a multivalent antimicrobial agent were identified. For additional comparison, samples for analysis of the wild type and mutated strains of B. cereus were prepared in both challenged and unchallenged conditions. A C16-DABCO (1,4‑diazabicyclo-2,2,2-octane) and mannose functionalized poly(amidoamine) dendrimer (DABCOMD) were used as the multivalent quaternary ammonium antimicrobial for this hydrophilic metabolic analysis. Overall, the study reported here indicates that B. cereus likely change their peptidoglycan layer to protect themselves from the highly positively charged DABCOMD. This membrane fortification most likely leads to the slow growth curve of the mutated, and especially the challenged mutant samples. The association of these sample types with metabolites associated with energy expenditure is attributed to the increased energy required for the membrane fortifications to occur as well as to the decreased diffusion of nutrients across the mutated membrane.

Novel Thermosensitive-co-Zwitterionic Sulfobetaine Gels for Metal Ion Removal: Synthesis and Characterization

Zwitterionic betaine polymers are promising adsorbents for the removal of heavy metal ions from industrial effluents. Although the presence of both negative and positively charged groups imparts them the ability to simultaneously remove cations and anions, intra- and/or inter-chain interactions can significantly reduce their adsorption efficiencies. Therefore, in this study, novel gels based on crosslinked co-polymers of thermosensitive N-isopropylacrylamide (NIPAAM) and zwitterionic sulfobetaine N,N-dimethylacrylamido propyl ammonium propane sulfonate (DMAAPS) were synthesized, characterized, and evaluated for ion removal. Fourier-transform infrared (FTIR) and proton nuclear magnetic resonance (1H NMR) analyses confirmed the success of the co-polymerization of NIPAAM and DMAAPS to form poly(NIPAAM-co-DMAAPS). The phase transition temperature of the co-polymer increased with increasing DMAAPS content in the co-polymer, indicating temperature-dependent amphiphilic behavior, as evidenced by contact angle measurements. The ion adsorption analyses of the poly(NIPAAM-co-DMAAPS) gels indicated that co-polymerization increased the molecular distance and weakened the interaction between the DMAAPS-charged groups (SO3− and N+), thereby increasing the ion adsorption. The results confirmed that, with a low concentration of DMAAPS in the co-polymer gels (~10%), the maximum amount of Cr3+ ions adsorbed onto the gel was ~58.49% of the sulfonate content in the gel.

Synthesis of a new furan-bearing triazine dichloride compound

Donor-acceptor compounds have been receiving increased attention lately, especially in opto-electronic applications. In this work, a novel compound named triazine-furan, comprised of a triazine acceptor moiety and a furan donor side group, was designed and synthesised for the first time. The influences of temperature and the feeding proportion of cyanuric chloride to furfurylamine were investigated to optimise the reaction yield and purification process. The synthesised compound was characterised using thin-layer chromatography (TLC), Fourier-transform infrared spectroscopy (FTIR), and proton nuclear magnetic resonance (1H-NMR) spectroscopy.

Exosome-Enriched Plasma Analysis as a Tool for the Early Detection of Hypertensive Gestations

Hypertensive disorders of pregnancy are closely associated with prematurity, stillbirth, and maternal morbidity and mortality. The onset of hypertensive disorders of pregnancy (HDP) is generally noticed after the 20th week of gestation, limiting earlier intervention. The placenta is directly responsible for modulating local and systemic physiology by communicating using mechanisms such as the release of extracellular vesicles, especially exosomes. In this study, we postulated that an analysis of exosome-enriched maternal plasma could provide a more focused and applicable approach for diagnosing HDP earlier in pregnancy. Therefore, the peripheral blood plasma of 24 pregnant women (11 controls, 13 HDP) was collected between 20th and 24th gestational weeks and centrifuged for exosome enrichment. Exosome-enriched plasma samples were analyzed by Raman spectroscopy and by proton nuclear magnetic resonance metabolomics (1H NMR). Principal component analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA) were used to analyze the Raman data, from the spectral region of 600–1,800 cm–1, to determine its potential to discriminate between groups. Using principal component analysis, we were able to differentiate the two groups, with 89% of all variances found in the first three principal components. In patients with HDP, most significant differences in Raman bands intensity were found for sphingomyelin, acetyl CoA, methionine, DNA, RNA, phenylalanine, tryptophan, carotenoids, tyrosine, arginine, leucine, amide I and III, and phospholipids. The 1H NMR analysis showed reduced levels of D-glucose, L-proline, L-tyrosine, glycine, and anserine in HDP, while levels of 2-hydroxyvalerate, polyunsaturated fatty acids, and very-low-density lipoprotein (VLDL) were increased. 1H NMR results were able to assign an unknown sample to either the control or HDP groups at a precision of 88.3% using orthogonal partial least squares discriminant analysis and 87% using logistic regression analysis. Our results suggested that an analysis of exosome-enriched plasma could provide an initial assessment of placental function at the maternal-fetal interface and aid HDP diagnosis, prognosis, and treatment, as well as to detect novel, early biomarkers for HDP.

1H Nuclear Magnetic Resonance: A Future Approach to the Metabolic Profiling of Psychedelics in Human Biofluids?

While psychedelics may have therapeutic potential for treating mental health disorders such as depression, further research is needed to better understand their biological effects and mechanisms of action when considering the development of future novel therapy approaches. Psychedelic research could potentially benefit from the integration of metabonomics by proton nuclear magnetic resonance (1H NMR) spectroscopy which is an analytical chemistry-based approach that can measure the breakdown of drugs into their metabolites and their metabolic consequences from various biofluids. We have performed a systematic review with the primary aim of exploring published literature where 1H NMR analysed psychedelic substances including psilocin, lysergic acid diethylamide (LSD), LSD derivatives, N,N-dimethyltryptamine (DMT), 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT) and bufotenin. The second aim was to assess the benefits and limitations of 1H NMR spectroscopy-based metabolomics as a tool in psychedelic research and the final aim was to explore potential future directions. We found that the most current use of 1H NMR in psychedelic research has been for the structural elucidation and analytical characterisation of psychedelic molecules and that no papers used 1H NMR in the metabolic profiling of biofluids, thus exposing a current research gap and the underuse of 1H NMR. The efficacy of 1H NMR spectroscopy was also compared to mass spectrometry, where both metabonomics techniques have previously shown to be appropriate for biofluid analysis in other applications. Additionally, potential future directions for psychedelic research were identified as real-time NMR, in vivo1H nuclear magnetic resonance spectroscopy (MRS) and 1H NMR studies of the gut microbiome. Further psychedelic studies need to be conducted that incorporate the use of 1H NMR spectroscopy in the analysis of metabolites both in the peripheral biofluids and in vivo to determine whether it will be an effective future approach for clinical and naturalistic research.

Synthesis, characterization and evaluation of stearyl acrylate-co-behenyl acrylate copolymer as a pour point depressant of waxy crude oil

Pour point depressant (PPD) has the competitive advantage of lowering the temperature of the wax appearance (WAT) and crude oil viscosity. In this paper, a novel PPD of poly stearyl acrylate-co-behenyl acrylate (SA-co-BA) in various mass ratios (1:1, 2:1, 3:1, 1:2 and 1:3) was effectively synthesized by solution radical polymerization method, and characterized by fourier transform infrared FTIR, proton nuclear magnetic resonance NMR, x-ray diffraction XRD and scanning electron microscopy SEM. The SA-co-BA PPD was evaluated on Malaysian crude oil via the pour point, the rheological and cold finger analysis to prevent the wax deposition at low temperature and improve flowability. The findings showed that the mass ratio (1:1) at 1000 ppm has a positive effect on the pour point depression from 11 to 2 °C. It was investigated from the rheological measurement that the viscosity of crude oil increases as the temperature decreases. Whereas, the viscosity decreases as the shear rate increases and as shear rate increases, shear stress increases. The flowability performance of the crude by the mass ratio of 1:1 at 1000 of the SA-co-BA concentrations have improved by 89.76%. The highest paraffin inhibition efficiency PIE of wax deposited was obtained at 1:1 of the mass ratio by 44.14%, indicating the smallest amount of wax is formed. This finding is interestingly attributed to the acrylate groups that have a long alkyl chain. Thus, SA-co-BA copolymer was demonstrated to be an appreciable pour point depressant that can prevent the wax deposition at low temperature and increasing the flowability of Malaysian crude oil.